Bioserenity is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Bioserenity - FDA 510(k) Cleared Devices
Recent clearances: Neuronaute with IceCap 2 & IceCap 2 Small
2
Total
2
Cleared
0
Denied
Bioserenity has 2 FDA 510(k) cleared medical devices. Based in Paris, FR.
Last cleared in 2023. Active since 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Bioserenity Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bioserenity
2 devices